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PMID: 2998053 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Transformation by polyoma ts-a mutants. I. Characterization of the transformed phenotype.

Virology ·Vol. 144 ·No. 2 ·1985-07-30 ·Pages 433-47

Winberry LK, Stewart CJ, Schaffhausen BS, Fluck MM

Abstract

Seven clonal lines of Fischer rat cells transformed with ts-a mutants of polyoma virus were studied. Four clones are characterized by a temperature-sensitive (ts) and three clones by a temperature-insensitive-transformed phenotype. Six clones have retained a functional though temperature-sensitive large T antigen, as judged by a 10- to 20-fold amplification of viral sequences in clones grown at low temperature compared to those grown at high temperature. No amplification is observed in one non-ts clone. As analyzed by Southern blotting, no obvious difference appears in the integration pattern of viral sequences in ts and non-ts clones concerning the number of sites of genome integration, the presence or absence of tandem repeats of the viral genome, or the absence of specific viral sequences. In autoradiograms of gel-electrophoresed immunoprecipitates, no correlation can be drawn between the amounts of either large T antigen or middle T antigen and the type of transformed state of the clones under the conditions tested. In assays of the middle T-antigen-associated kinase, no reproducible difference can be observed between the non-ts and ts clones. Finally, no correlation was observed between a temperature-insensitive phenotype and the production of an N-terminal fragment of large T antigen. Thus the molecular basis for the difference between ts-a transformants with ts or non-ts phenotypes remains elusive.

MeSH Terms
Antigens, Viral, Tumor/genetics Cell Transformation, Viral DNA, Viral/genetics Gene Amplification Gene Expression Regulation Genetic Linkage Mutation Phenotype Polyomavirus/genetics Protein Kinases/genetics Repetitive Sequences, Nucleic Acid Temperature
Chemicals
Antigens, Viral, Tumor DNA, Viral Protein Kinases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Winberry L K
Stewart C J
Schaffhausen B S
Fluck M M
Article Info
Journal
Virology
Abbr.
Virology
ISSN
0042-6822
Published
1985-07-30
Pages
433-47
Language
English
Region
United States
NLM ID
0110674
Subset
IM
Grants
NCI NIH HHS · R01 CA034722 · United States
NCI NIH HHS · R01 CA 29270 · United States
NCI NIH HHS · R01 CA 34722 · United States
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